SCN1A c.475T>C ;(p.Y159H)

Variant ID: 2-166911275-A-G

NM_001165963.1(SCN1A):c.475T>C;(p.Y159H)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Genetic Diagnosis in Children with Epilepsy and Developmental Disorders by Targeted Gene Panel Analysis in a Developing Country.

Journal Of Epilepsy Research
Rahman, Md Mizanur MM; Fatema, Kanij K
Publication Date: 2021-06

Variant appearance in text: SCN1A: 475T>C; Tyr159His
PubMed Link: 34395220
Variant Present in the following documents:
  • Main text
  • jer-21004.pdf
View BVdb publication page